Evidence map›Paper›PMID 42516382›Full record

ArticleFrontiers in immunology2026

Clinical and PET/CT metabolic imaging characteristics across the evolving spectrum of visceral leishmaniasis and associated hemophagocytic lymphohistiocytosis.

Chao Yang, Yan Wang, Ruixian Duan, Feiyan Wei, Xiu Sun

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Chao Yang *Department of Infection, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.
Yan Wang *Department of Infection, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.
Ruixian DuanDepartment of Infection, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.
Feiyan WeiDepartment of Infection, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.
Xiu SunDepartment of Infection, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To delineate the clinical and PET/CT metabolic imaging characteristics across the spectrum of visceral leishmaniasis(VL) and associated hemophagocytic lymphohistiocytosis (HLH), and to develop a simple risk score for identification of patients at risk of visceral leishmaniasis-associated hemophagocytic lymphohistiocytosis (VL-HLH). Methods: This retrospective study enrolled 21 VL patients categorized into three groups: visceral leishmaniasis only (VL-only, n=7), VL-HLH (n=8), and a clinically indeterminate Grey Zone group (n=6). Clinical and laboratory parameters were compared across groups. For 9 patients with PET/CT, metabolic patterns and correlations between splenic SUVmax and serological markers were analyzed. A simple risk score was constructed based on significant indicators and evaluated across groups. Results: No differences were observed in age, sex, and main symptoms among the three groups. Compared to the VL-only group, the VL-HLH group exhibited significantly higher levels of the inflammatory marker C-reactive protein and greater spleen thickness (P<0.05). Correlation analysis revealed a multi-indicator interaction network centered on "inflammation-coagulation-tissue injury." PET/CT identified the spleen (9/9, 100%) and bone marrow (7/9, 77.8%) as the primary metabolic target organs; splenic SUVmax showed strong positive correlations with D-dimer (r=0.82, p<0.01) and ferritin (r=0.69, p<0.05). The simple risk stratification tool (0-2 points) based on C-reactive protein and spleen thickness demonstrated a clear discriminative trend: the VL-only group concentrated at 0 points (85.7%), while the VL-HLH group distributed across 1-2 points. The Jonckheere-Terpstra test for trend confirmed a statistically significant increasing trend in scores with greater disease severity (from VL-only, to Grey Zone, to VL-HLH) (P = 0.002). Conclusion: This study reveals a systemic "inflammation-coagulation-tissue injury" network in VL, with the spleen as its core metabolic targets. The proposed simple stratification tool based on C-reactive protein and spleen thickness serves as a practical instrument for clinical risk warning.

Indexed as

Leishmaniasis, VisceralLymphohistiocytosis, HemophagocyticPositron Emission Tomography Computed TomographyAdolescentAdultBiomarkersChildChild, PreschoolFemaleHumansMaleRetrospective StudiesSpleenYoung AdultBiomarkershemophagocytic lymphohistiocytosismetabolic imagingpositron emission tomographyrisk stratificationvisceral leishmaniasis

Identifiers

PMID42516382
PMCPMC13402202

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.